Canonical Allele Identifier: CA416904392

Gene: FABP3

Linked Data

• MyVariant Identifiers: chr1:g.31845856C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31373009C>T , CM000663.2:g.31373009C>T	GRCh38
NC_000001.10:g.31845856C>T , CM000663.1:g.31845856C>T	GRCh37
NC_000001.9:g.31618443C>T	NCBI36
NG_047049.1:g.5275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.6G>A MANE Select	ENSP00000362817.2:p.Val2=
ENST00000373713.6:c.6G>A	ENSP00000362817.2:p.Val2=
ENST00000482018.1:c.6G>A	ENSP00000473982.1:p.Val2=
ENST00000498148.5:c.6G>A	ENSP00000474078.1:p.Val2=
NM_004102.3:c.6G>A	NP_004093.1:p.Val2=
XM_011541007.1:c.6G>A	XP_011539309.1:p.Val2=
NM_001320996.1:c.6G>A	NP_001307925.1:p.Val2=
NM_004102.4:c.6G>A	NP_004093.1:p.Val2=
XM_011541007.3:c.6G>A	XP_011539309.1:p.Val2=
NM_004102.5:c.6G>A MANE Select	NP_004093.1:p.Val2=
NM_001320996.2:c.6G>A	NP_001307925.1:p.Val2=